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total trka  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc total trka
    Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting <t>analysis.</t> <t>Tyr674/675</t> <t>phospho-TrkA</t> indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.
    Total Trka, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 244 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/total trka/product/Cell Signaling Technology Inc
    Average 95 stars, based on 244 article reviews
    total trka - by Bioz Stars, 2026-03
    95/100 stars

    Images

    1) Product Images from "NGF promotes cell cycle progression by regulating D-type cyclins via PI3K/Akt and MAPK/Erk activation in human corneal epithelial cells"

    Article Title: NGF promotes cell cycle progression by regulating D-type cyclins via PI3K/Akt and MAPK/Erk activation in human corneal epithelial cells

    Journal: Molecular Vision

    doi:

    Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting analysis. Tyr674/675 phospho-TrkA indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.
    Figure Legend Snippet: Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting analysis. Tyr674/675 phospho-TrkA indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.

    Techniques Used: Incubation, Expressing, Western Blot, Activity Assay



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    Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting <t>analysis.</t> <t>Tyr674/675</t> <t>phospho-TrkA</t> indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.
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    Cell Signaling Technology Inc rabbit anti total trka
    Fig. 8 Effects of SCH and OHT on NGF-mediated <t>TrkA</t> and p75NTR signaling pathway. NGF induces TrkA signaling pathway to increase neuronal prolifera- tion. Pro-NGF, the precursor protein of NGF, can combine with p75NTR preferentially to enhance neuronal apopto- sis. CREB, cAMP response element-binding protein; JNK, C-Jun N-terminal kinase; NGF, nerve growth factor; OHT, overt hypothyroidism; p75NTR, p75 neurotrophin receptor; SCH, subclinical hypothyroidism; TrkA, tropomyosin-related kinase A
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    Image Search Results


    Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting analysis. Tyr674/675 phospho-TrkA indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.

    Journal: Molecular Vision

    Article Title: NGF promotes cell cycle progression by regulating D-type cyclins via PI3K/Akt and MAPK/Erk activation in human corneal epithelial cells

    doi:

    Figure Lengend Snippet: Effect of nerve growth factor on the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) and mitogen activated protein kinase (MAPK)/extracellular signal-regulated kinase (Erk) signaling pathways in human corneal epithelial cells. A : Human corneal epithelial cells (HCECs) were incubated in defined keratinocyte serum-free medium (K-SFM) without growth factors for 24 h before nerve growth factor (NGF) stimulation and then treated with NGF at 25 ng/ml for different periods. B : HCECs were treated with different concentrations of NGF for 60 min. A total of 50 μg cell lysates were analyzed for expression of the indicated genes by immunoblotting analysis. Tyr674/675 phospho-TrkA indicates the NGF signaling activity. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as a loading control. For both A and B , results are representative of three independent experiments. Experiments were performed in triplicate.

    Article Snippet: Antibodies against Tyr674/675 phospho-TrkA, total TrkA, Ser473 phospho-Akt, total Akt, Thr202/Tyr204 phospho-p44/42 MAPK (Erk1/2), total p44/42 MAPK (Erk1/2), cyclin D2, and anti-Rabbit IgG HRP-conjugated Secondary Antibody were from Cell Signaling Technology (Beverly, MA).

    Techniques: Incubation, Expressing, Western Blot, Activity Assay

    Fig. 8 Effects of SCH and OHT on NGF-mediated TrkA and p75NTR signaling pathway. NGF induces TrkA signaling pathway to increase neuronal prolifera- tion. Pro-NGF, the precursor protein of NGF, can combine with p75NTR preferentially to enhance neuronal apopto- sis. CREB, cAMP response element-binding protein; JNK, C-Jun N-terminal kinase; NGF, nerve growth factor; OHT, overt hypothyroidism; p75NTR, p75 neurotrophin receptor; SCH, subclinical hypothyroidism; TrkA, tropomyosin-related kinase A

    Journal: Molecular neurobiology

    Article Title: Maternal Subclinical Hypothyroidism in Rats Impairs Spatial Learning and Memory in Offspring by Disrupting Balance of the TrkA/p75 NTR Signal Pathway.

    doi: 10.1007/s12035-021-02403-z

    Figure Lengend Snippet: Fig. 8 Effects of SCH and OHT on NGF-mediated TrkA and p75NTR signaling pathway. NGF induces TrkA signaling pathway to increase neuronal prolifera- tion. Pro-NGF, the precursor protein of NGF, can combine with p75NTR preferentially to enhance neuronal apopto- sis. CREB, cAMP response element-binding protein; JNK, C-Jun N-terminal kinase; NGF, nerve growth factor; OHT, overt hypothyroidism; p75NTR, p75 neurotrophin receptor; SCH, subclinical hypothyroidism; TrkA, tropomyosin-related kinase A

    Article Snippet: The membranes were incubated overnight at 4 °C with the following antibodies: rabbit anti-NGF (1:1000 dilution; Abcam, ab52918, Cambridgeshire, UK); rabbit anti-proNGF (1:1000 dilution; Sigma-Aldrich, P5498); rabbit anti-total TrkA (1:1000 dilution; Cell Signaling Technology 2505S, USA); rabbit anti-p-TrkA (1:1000 dilution; Abcam, ab1445); rabbit anti-total ERK (1:1000 dilution; CST4695S); rabbit anti-pERK (1:2000 dilution; CST4370S); rabbit anti-total CREB (1:1000 dilution; CST9197S); rabbit anti-p-CREB (1:1000 dilution; CST9198S); rabbit anti-p75NTR (1:1000 dilution; CST8238S); rabbit anti-p53 (1:1000 dilution; CST32532S); rabbit anti-total JNK (1:1000 dilution; CST9252S); rabbit anti-p-JNK (1:1000 dilution; CST4668S); rabbit anti-Bax (1:1000 dilution; CST2772S); and rabbit anti-cleaved caspase-3 (1:1000 dilution; CST9664S).

    Techniques: Binding Assay